Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1006737
rs1006737
25 0.695 0.120 12 2236129 intron variant G/A snv 0.36 0.900 0.917 10 2010 2016
dbSNP: rs4765905
rs4765905
6 0.827 0.040 12 2240418 intron variant G/A;C snv 0.710 1.000 1 2011 2016
dbSNP: rs2239073
rs2239073
1 1.000 0.040 12 2429334 intron variant T/C snv 0.50 0.010 1.000 1 2016 2016
dbSNP: rs4765937
rs4765937
1 1.000 0.040 12 2461369 intron variant T/C snv 0.42 0.010 1.000 1 2016 2016
dbSNP: rs794727961
rs794727961
5 0.851 0.080 12 2512979 missense variant G/A snv 0.010 1.000 1 2010 2010